Labeling errors are a recurring reality for medical devices. Companies’ continued reliance on manual processes and incongruent labeling systems often results in pricey product recalls. As label content becomes more complex with the introduction of new regulations, costs to change global labels will increase if companies don’t proactively review and strengthen their labeling infrastructure. This eBook discusses the four most common scenarios in recalling labeled medical device products and solutions for each of them. Download the full eBook for more information.